Methods of synthesizing 2-substituted-1,4-benzenediamine
View Patent ↗Disclosed is a method of making a 2-substituted-1,4-benzenediamine by nucleophilic aromatic substitution.
1. A method for making 2-substituted-1,4-benzenediamine comprising:
(a) introducing ammonia to a 4-nitro-2-(or 3-)substituted-chlorobenzene to obtain a 4-nitro-2-(or 3-)substituted-aminobenzene:
(b) hydrogenating the 4-nitro-2-(or 3-) substituted-aminobenzene in the presence of an hydrogenation catalyst to form a 2-substituted-1,4-benzenediamine:
wherein X of formulae (I)-(III)) is selected from the group consisting of:
(a) a branched alkyl;
(b) methoxy, ethoxy, propoxy, isopropoxy, butoxy;
(c) C1-C6 alkyl or branched alkyl with hydroxy substitution;
(d) —(CH2)yOCH3; wherein y is from 1-3;
(e) —(CH2)yOCH2CH3; wherein y is from 1-3;
(f) —(CH2)yOCH2CH2CH3; wherein y is from 1-3;
wherein Z is hydrogen or C1-3 alkyl; and
(h) mixtures thereof.
2. The method of claim 1 , wherein the hydrogenation catalyst is palladium based, platinum based, or nickel based.
3. The method of claim 1 , wherein the hydrogenating step occurs in an hydrogenation solvent selected from a group consisting of ethyl acetate, toluene, butyl acetate, ethanol and methanol.
4. The method of claim 1 wherein the hydrogenating step further comprises applying a hydrogen atmosphere of about 446 to about 515 kPa pressure.
5. The method of claim 1 wherein the hydrogenating step further comprises heating under an atmosphere of hydrogen to a temperature within a range of about 20° C. to about 80° C.
6. The method of claim 1 , wherein the method does not comprise a purification step.
7. The method of claim 1 wherein the introducing ammonia step is in a stirred reactor further comprising charging the reactor with nitrogen to a pressure which is within a range of between about 618 kPa and 791 kPa, heating the mixture to a temperature within a range of about 150° C. to about 220° C. and stirring the mixture at this temperature for a time period of about 1 hour to about 24 hours.
8. The method of claim 1 wherein the introducing ammonia step is carried out in a solvent selected from formamide or acetonitrile.
9. A method for making 2-substituted-1,4-benzenediamine comprising:
(a) introducing ammonia to 4-nitro-2-substituted-chlorobenzene to obtain 4-nitro-2-substituted-aminobenzene:
(b) hydrogenating the 4-nitro-2-substituted-aminobenzene in the presence of a hydrogenation catalyst to form a 2-substituted-1,4-benzenediamine
wherein X of formulae (Ia), (IIa) and (III) is selected from the group consisting of:
(b) methoxy, ethoxy, propoxy, isopropoxy, butoxy;
(c) a C1-C6 alkyl with hydroxy substitution;
(d) —(CH2)yOCH3; wherein y is from 1-3;
(e) —(CH2)yOCH2CH3; wherein y is from 1-3;
(f) —(CH2)yOCH2CH2CH3; y is from 1-3;
wherein Z is hydrogen or C1-3 alkyl; and
(h) mixtures thereof.
10. A method for making 2-substituted-1,4-benzenediamine comprising:
(a) introducing ammonia to 4-nitro-3-substituted-chlorobenzene to obtain 4-nitro-3-substituted-aminobenzene:
(b) hydrogenating the 4-nitro-3-substituted-aminobenzene in the presence of a hydrogenation catalyst to form a 2-substituted-1,4-benzenediamine:
wherein X of formulae (Ib), (IIb) and (III) is selected from the group consisting of:
(b) methoxy, ethoxy, propoxy, isopropoxy, butoxy
(c) a C1-C6 alkyl with hydroxy substitution;
(d) —(CH2)yOCH3; wherein y is from 1-3;
(e) —(CH2)yOCH2CH3; wherein y is from 1-3;
(f) —(CH2)yOCH2CH2CH3; wherein y is from 1-3;
wherein Z is hydrogen or C1-3 alkyl; and
(h) mixtures thereof.
11. The method of claim 1 , wherein the method further comprises a step before introducing ammonia step, said step comprising introducing a 4-nitro-2 (or 3-) substituted chlorobenzene to an alkyl halide which results in the 4-nitro-2-(or 3-) substituted-chlorobenzene;
wherein X 2 of formula (XI) is selected from the group consisting of —(CH2)yOH;
y is from 1-3;
and mixtures thereof; wherein Y of the Yhalide can be a C1-C4 alkyl; and the halide is a halogen;
wherein X of formula (I) is selected from the group consisting of: (d) —(CH2)yOCH3; y is from 1-3 (e) —(CH2)yOCH2CH3; y is from 1-3 (f) —(CH2)yOCH2CH2CH3; y is from 1-3
Z C1-C4 alkyl; and mixtures thereof; the base is selected from a suitable alkali alkoxides, alkali hydroxide; and mixtures thereof.
12. The method of claim 11 , wherein the ether forming agent is introduced to a 4-nitro-2-haloalkyl substituted chlorobenzene to result in the 4-nitro-2-substituted-chlorobenzene:
wherein X 2 of formula (XIa) is selected from the group consisting of —(CH2)yOH; y is from 1-3;
and mixtures thereof; wherein Y of the Yhalide can be a C1-C4 alkyl; wherein “halide” of the Yhalide may be a halogen, such as F, Cl or Br; wherein X of formula (Ia) is selected from the group consisting of: (d) —(CH2)yOCH3; y is from 1-3 (e) —(CH2)yOCH2CH3; y is from 1-3 (f) —(CH2)yOCH2CH2CH3; y is from 1-3
Z is C1-C3 alkyl; and mixtures thereof; the base is selected from a suitable alkali alkoxides, alkali hydroxide and mixtures thereof.
13. The method of claim 11 , wherein the ether forming agent is introduced to a 4-nitro-3-haloalkyl substituted chlorobenzene to result in the 4-nitro-3-substituted-chlorobenzene:
wherein X 2 of formula (XIb) is selected from the group consisting of —(CH2)yOH; y is from 1-3;
and mixtures thereof;
wherein X of formula (Ib) is selected from the group consisting of: (d) —(CH2)yOCH3; y is from 1-3 (e) —(CH2)yOCH2CH3; y is from 1-3 (f) —(CH2)yOCH2CH2CH3; y is from 1-3
Z is C1-C3 alkyl; and mixtures thereof; Y of the Yhalide can be a C1-C4 alkyl, the halide of the Yhalide may be a halogen, such as F, Cl or Br and wherein the base is selected from a suitable alkali alkoxides, alkali hydroxide and mixtures thereof.
14. The method of claim 1 wherein the method further comprises a step after the hydrogenation step comprising precipitating, with an acid solution comprising a reductant, a salt of the 2-substituted-1,4-benzenediamine.
15. The method of claim 14 wherein the precipitating step further comprises cooling to maintain the reaction at a temperature within a range of about 0° C. to about 40° C., more typically about 10° C. to about 30° C., over a period of about 30 minutes to 3 hours until the salt of the 2-substituted-1,4-benzenediamine crystallizes out of the solution.
16. The method of claim 14 wherein the acid solution comprises an acid selected from the group consisting of malic acid, sulfuric acid, hydrochloric acid, phosphoric acid, tartaric acid and mixtures thereof.
17. The method of claim 14 wherein the precipitation step further comprises filtering, washing and drying the salt of the 2-substituted-1,4-benzenediamine.
18. A method of making 2-methoxymethyl-1,4-benzenediamine comprising the steps:
a) introducing ammonia to a 4-nitro-2-(or 3-)methoxymethylchlorobenzene to obtain 4-nitro-2-(or 3-) methoxymethyl-aminobenzene; and
b) hydrogenating the 4-nitro-2-(or 3-)methoxymethyl-aminobenzene in the presence of a hydrogenation catalyst to obtain the 2-methoxymethyl-1,4-benzenediamine.
19. The method of claim 18 wherein the method further comprises a step before the introducing ammonia step, said further step comprising introducing a methoxy group to the 4-nitro-2-(or 3-) chloromethylchlorobenzene to obtain 4-nitro-2-(or 3-) methoxymethylchlorobenzene.
20. The method of claim 18 wherein the method further comprises a step of exchanging the chloro atom of the 4-nitro-2-(or 3-) methoxymethylchlorobenzene with a fluoro atom, wherein the exchange is completed before the introducing ammonia step or during the step of introducing ammonia.
21. The method of claim 18 wherein the method further comprises a step before the introducing ammonia step, said further step comprising brominating a 4-nitro-2 (or 3-) hydroxymethylchlorobenzene then introducing a methoxy group to obtain the 4-nitro-2-(or 3-) methoxymethylchlorobenzene.
22. A method of making 2-methoxymethyl-1,4-benzenediamine comprising the steps:
a) nitrating 2-(or 3-) halobenzylhalide to obtain 4-nitro-2-(or 3-) halomethylhalobenzene;
b) introducing a methoxy group to the 4-nitro-2-(or 3-) halomethylhalobenzene to obtain 4-nitro-2-(or 3-) methoxymethylhalobenzene;
c) introducing ammonia to the 4-nitro-2-(or 3-) methoxymethylhalobenzene to obtain 4-nitro-2-(or 3-) methoxymethyl-aminobenzene; and
d) hydrogenating the 4-nitro-2-(or 3-) methoxymethyl-aminobenzene in the presence of a hydrogenation catalyst to obtain the 2-methoxymethyl-1,4-benzenediamine.
23. The method of claim 22 wherein the 3-halobenzylhalide, the 4-nitro-2-(or 3-) halomethylhalobenzene and the 4-nitro-2-(or 3-) methoxymethylhalobenzene are
selected to be 2-(or 3-) chlorobenzylchloride, 4-nitro-2-(or 3-) chloromethylchlorobenzene and 4-nitro-2-(or 3-) methoxymethylchlorobenzene.